The Attached and Train raining period lasts for 15 months. Structured on-the-job training (OJT) will be provided and conducted at the participating companies to facilitate the application of learning and to ensure that individuals acquire necessary competencies to perform at their job.

The trainee will support day-to-day operations within a GMP-regulated manufacturing environment. The role involves performing tasks that contribute to the efficient, compliant, and safe operation of the assigned department while adhering to company policies, procedures, and applicable regulatory requirements.

This is a fully site‑based role at Singapore Tuas. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. The role follows regular office working hours (Monday to Friday).

What you’ll get:

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Daily company bus from the MRT location near your home to and from the Tuas site.

What you'll do

• Learn and apply GMP principles, company policies, and Standard Operating Procedures (SOPs) in daily activities.
• Support routine operations within assigned departments while maintaining compliance with quality, safety, and regulatory requirements.
• Assist with documentation, data entry, record review, and maintenance of GMP documents such as logbooks, batch records, and reports.
• Perform basic laboratory, manufacturing, or technical tasks under supervision, depending on the assigned department.
• Support equipment monitoring, routine inspections, housekeeping (6S), and workplace organization.
• Participate in sample collection, testing, investigations, or process monitoring activities where applicable.
• Assist with equipment qualification, validation, technology transfer, process improvement, or continuous improvement initiatives as assigned.
• Learn to identify, report, and support the resolution of deviations, non-conformances, and corrective and preventive actions (CAPA).
• Develop an understanding of manufacturing processes, quality systems, and regulatory requirements applicable to pharmaceutical operations.
• Use electronic systems such as Laboratory Information Management Systems (LIMS), Manufacturing Execution Systems (MES), Enterprise Resource Planning (ERP), or other digital platforms where applicable.
• Collaborate effectively with cross-functional teams to support operational objectives and project activities.
• Participate in departmental meetings, training programmes, audits, and compliance initiatives.

What we’re looking for:

• Diploma/ Degree in relevant science discipline (Biotechnology, Pharmaceutical Sciences, Biomedical Engineering etc.)

• Strong interpersonal skills

• Effective verbal and written communication skills

• Meticulous eye for detail

• Systematic

• Positive team player

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.